Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Очень мало
$65к-75к/год
$84к$98кмедиана$110к
По похожим ролям (50) ~ $98к/год
На СНГ рынке: $1.8к/мес ($1.4к - $3к)
58
Средняя вакансия
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Это понятная руководящая роль в клинических исследованиях у известного университета с хорошим соцпакетом, но зарплата $65 000-$75 000 заметно ниже рыночного ориентира, а грантовый контракт ограничен пятью годами.
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Ниже рынкаКонтракт до пяти летПонятная зона ответственностиХороший соцпакет
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Project Manager I (Clinical Research): Managing a federally funded, five-year clinical research study with an accent on regulatory oversight, multi-site protocol implementation, participant coordination, and research data quality. Focus on maintaining human-subjects compliance, supervising study personnel, coordinating digital health assessments, and resolving operational issues across collaborating institutions.
Location: On-site in Tampa, Florida, United States
Salary: $65,000–$75,000 per year
Company
hirify.global is a public research university with extensive federally funded research activity and health sciences programs.
What you will do
Manage daily operations for a federally funded, five-year clinical research study.
Coordinate participant recruitment, screening, enrollment, informed consent, study visits, retention, and follow-up assessments.
Prepare and maintain IRB submissions, amendments, continuing reviews, adverse event reports, protocol deviations, and regulatory correspondence.
Implement study protocols across multiple research sites and oversee participant assessments, intervention delivery, data collection, and study supplies.
Maintain quality assurance and data quality procedures, prepare safety monitoring reports, and recommend process improvements.
Recruit, train, supervise, and evaluate research nurses, health coaches, student workers, research assistants, and volunteers.
Requirements
Bachelor’s degree in a related field and at least two years of project management or coordination experience; four years of direct experience may substitute for the degree.
Employment eligibility requirements in the United States must be met.
Knowledge of human-subjects research regulations, Good Clinical Practice, and Institutional Review Board processes.
Experience with project coordination, organization, leadership, communication, and multi-site collaboration.
Ability to manage regulatory documentation, participant safety, protocol fidelity, research data, and operational reporting.
Ability to work on-site in Tampa and supervise study personnel.
Nice to have
Master’s degree in Nursing, Public Health, Health Sciences, Exercise Science, Psychology, or a related health field.
Experience coordinating federally funded clinical, behavioral, or translational research studies.
Experience with cardiovascular disease populations, women’s health research, and studies from initiation through closeout.
ACRP, SOCRA, or equivalent professional research certification.
Experience with electronic health records, REDCap, and electronic data capture systems.
Culture & Benefits
Grant-funded, time-limited position with a contract of up to five years.
Medical, dental, and life insurance plans.
Retirement plan options and generous leave.
Employee and dependent tuition programs.
Additional employee perks and discounts.
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